Canonical Allele Identifier: CA1752445310

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150977285A= , CM000669.2:g.150977285A=	GRCh38
NC_000007.13:g.150674373A= , CM000669.1:g.150674373A=	GRCh37
NC_000007.12:g.150305306A=	NCBI36
NG_008916.1:g.5642T= , LRG_288:g.5642T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262186.10:c.76+553T= MANE Select	ENSP00000262186.5:n.76+553T=
ENST00000262186.9:c.76+553T=	ENSP00000262186.5:n.76+553T=
ENST00000430723.4:c.-102+553T=	ENSP00000387657.4:n.-102+553T=
ENST00000532957.5:n.299+553T=
NM_000238.3:c.76+553T= , LRG_288t1:c.76+553T=	NP_000229.1:n.76+553T=
NM_172056.2:c.76+553T= , LRG_288t2:c.76+553T=	NP_742053.1:n.76+553T=
XM_011516186.1:c.76+553T=	XP_011514488.1:n.76+553T=
XM_011516186.3:c.76+553T=	XP_011514488.1:n.76+553T=
NM_000238.4:c.76+553T= MANE Select	NP_000229.1:n.76+553T=